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• W3119495065 endingPage "76" @default.
• W3119495065 startingPage "67" @default.
• W3119495065 abstract "The identification of C9orf72 gene has led to important scientific progresses and has considerably changed our clinical practice. However, a decade after C9orf72 discovery, some important clinical questions remain unsolved. The reliable cutoff for the pathogenic repeat number and the implication of intermediate alleles in frontotemporal dementia, amyotrophic lateral sclerosis, or in other diseases are still uncertain. The occurrence of an anticipation phenomenon - at the clinical and molecular levels - in C9orf72 kindreds is still debated as well, and the factors driving age at onset and phenotype variability are largely unknown. All these questions have a significant impact not only in clinical practice for diagnosis and genetic counseling but also in a research context for the initiation of therapeutic trials. In this chapter, we will address all those issues and summarize the recent updates about clinical aspects of C9orf72 disease, focusing on both the common and the less typical phenotypes." @default.
• W3119495065 created "2021-01-18" @default.
• W3119495065 creator A5042566383 @default.
• W3119495065 creator A5063744167 @default.
• W3119495065 date "2021-01-01" @default.
• W3119495065 modified "2023-09-24" @default.
• W3119495065 title "Clinical Update on C9orf72: Frontotemporal Dementia, Amyotrophic Lateral Sclerosis, and Beyond" @default.
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